A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577953



Internal ID21526413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103234872..103237431hg38UCSC Ensembl
chr7:102875319..102877878hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382560
hg192560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150748
SamplesHG00513
Known GenesDPY19L2P2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577953
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer